Organic zwitterions
4-Nitro-1H-pyrazole-3-carboxylic acid, 98%, Thermo Scientific Chemicals
CAS: 5334-40-7 Molecular Formula: C4H3N3O4 Molecular Weight (g/mol): 157.085 MDL Number: MFCD00090899 InChI Key: ZMAXXOYJWZZQBK-UHFFFAOYSA-N Synonym: 4-nitro-1h-pyrazole-3-carboxylic acid,4-nitropyrazole-3-carboxylic acid,4-nitro-3-pyrazolecarboxylic acid,4-nitro-1h-pyrazole-5-carboxylic acid,1h-pyrazole-3-carboxylic acid, 4-nitro,4-nitro-2h-pyrazole-3-carboxylic acid,4-nitro pyrazole-3-carboxylic acid,4-nitro-pyrazole-3-carboxylic acid,4-hydroxynitroso-1h-pyrazole-3-carboxylic acid,nitropyrazolecarboxylic PubChem CID: 219739 SMILES: C1=NNC(=C1[N+](=O)[O-])C(=O)O
Sigma Aldrich 3-amino-pentanoic acid
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 4-(1-(hydroxymethyl)cyclopropyl)phenylboronic acid
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 5-(4-Nitrophenyl)thiophene-2-carboxylic acid
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 4-Hydroxy-6-methylquinoline-3-carboxylic acid
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 5-Oxo-5,6,7,8-tetrahydro-2-naphthalenecarboxylic acid
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Zinc N-Ethyl-N-phenyldithiocarbamate 98.0+%, TCI America™
CAS: 14634-93-6 Molecular Formula: C18H20N2S4Zn Molecular Weight (g/mol): 457.992 MDL Number: MFCD00059686 InChI Key: KMNUDJAXRXUZQS-UHFFFAOYSA-L Synonym: N-Ethyl-N-phenyldithiocarbamic Acid Zinc Salt PubChem CID: 6093375 IUPAC Name: zinc;N-ethyl-N-phenylcarbamodithioate SMILES: CCN(C1=CC=CC=C1)C(=S)[S-].CCN(C1=CC=CC=C1)C(=S)[S-].[Zn+2]
Accela Chembio Inc 4-nitropyrazole-3-carboxylic Acid | 25g | 5334-40-7 | MFCD00090899 | 98% | Shelf Life: 900 Days | Light Sensitive
4-nitropyrazole-3-carboxylic Acid | 25g | 5334-40-7 | MFCD00090899 | 98% | Shelf Life: 900 Days | Light Sensitive
Cayman Chemical Arachidonoyl pNitroaniline
ApNA is one of several nitroaniline fatty acid amides which can be used to measure FAAH activity.{8928} FAAH is a relatively unselective enzyme in that it accepts a variety of amide head groups other than the ethanolamine of its nominal endogenous substrate AEA (Item No. 90050). It also will hydrolyze fatty acid amides with fewer carbons and fewer double bonds than arachidonate. (See also Decanoyl p-Nitroaniline - Catalog No. 90349). Exposure of ApNA to FAAH activity results in the release of the yellow colorimetric dye p-nitroaniline (ε = 13,500 at 382 nm). This offers the potential for fast and convenient measurements of FAAH activity using a 96-well plate spectrophotometer.
N-n-Hexyl-3,5-dinitrobenzamide, 97%, Thermo Scientific™
CAS: 92043-81-7 Molecular Formula: C13H17N3O5 Molecular Weight (g/mol): 295.295 MDL Number: MFCD00413284 InChI Key: ULUBCUUBHVXVDB-UHFFFAOYSA-N Synonym: n-n-hexyl-3,5-dinitrobenzamide,3,5-dinitrophenyl-n-hexylcarboxamide,3-hexylcarbamoyl-5-hydroxyazonoyl-phenyl azinic acid PubChem CID: 4456526 IUPAC Name: N-hexyl-3,5-dinitrobenzamide SMILES: CCCCCCNC(=O)C1=CC(=CC(=C1)[N+](=O)[O-])[N+](=O)[O-]